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Article

Studying the Association between Sudden Hearing Loss and DNA N-Methyltransferase 1 (DNMT1) Genetic Polymorphism.

The journal of international advanced otology - 1 Dec 2017

Şeker Yıldız Kübra, Durmuş Kasım, Dönmez Gonca, Arslan Serdal, Altuntaş Emine Elif

Abstract excerpt

OBJECTIVE: The aim of the present study was to investigate whether there was any relationship between some DNA N-methyltransferase 1 (DNMT1) polymorphisms and susceptibility to idiopathic sudden sensorineural hearing loss (ISSHL) in ISSHL patients. MATERIAL AND METHODS: We investigated 90 patients diagnosed with ISSHL and a control group composed of 75 age- and gender-matched healthy individuals. DNA was...

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Source

Identifiers

PMID: 28414276
DOI: 10.5152/iao.2017.2723

Genes

DNMT1
GAA

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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